ライフサイエンスコーパス: xenogeneic

1 accomplished by grafting only the SDRs of a xenogeneic Ab onto human Ab frameworks.

2 In a xenogeneic adoptive transfer model, we have compared the

3 term metabolic function of microencapsulated xenogeneic adult porcine islets (API) was assessed in a

4 ing improved regression of human cancer in a xenogeneic allograft model.

5 When rejection occurred on days 4 and 8 in xenogeneic and allogeneic recipients, 60% (57-68) and 55

6 human regulatory T cells (Tregs) to suppress xenogeneic and allogeneic responses in vitro.

7 hESC(siRNA+IB) was strongly reduced in both xenogeneic and allogeneic settings.

8 exhibit compromised rejection of allogeneic, xenogeneic and missing self bone-marrow grafts.

9 At 2 days, injection sites of xenogeneic and syngeneic cells (cardiac-derived stem cel

10 at are capable of killing a large variety of xenogeneic and syngeneic cells.

11 possibility of imaging inflammation in both xenogeneic and syngeneic tumor models, which resulted in

12 We estimated the decrease in expression of a xenogeneic antigen, Galalpha1-3Gal, which might be neede

13 ced in xenograft recipients against multiple xenogeneic antigens.

14 ursor experiments have been carried out in a xenogeneic background in order to utilize species-specif

15 licited immune response of healthy dogs to a xenogeneic BAL was blocked and BAL performance significa

16 o induce tolerance across a highly disparate xenogeneic barrier has not yet been demonstrated.

17 wo strategies to induce tolerance across the xenogeneic barrier, namely thymus transplantation and mi

18 olerance across a discordant (pig-to-baboon) xenogeneic barrier.

19 survival across the discordant pig-to-baboon xenogeneic barrier.

20 ial, but also to understanding the nature of xenogeneic barriers and mechanisms of heterochronicity,

21 nsplantation because immune responses across xenogeneic barriers are vigorous.

22 e transplant tolerance across allogeneic and xenogeneic barriers, and to support long-term thymopoies

23 ucing T cell tolerance across allogeneic and xenogeneic barriers.

24 mouse) and highly disparate (pig to rodent) xenogeneic barriers.

25 ion across allogeneic and potentially across xenogeneic barriers.

26 success of transplants across allogeneic and xenogeneic barriers.

27 nts of antigenicity in a clinically relevant xenogeneic biomaterial (i.e. BP) and further validates a

28 onstrate that anti-CD40L in combination with xenogeneic BMT can tolerize preexisting peripheral and i

29 Mixed xenogeneic bone marrow chimeras resulting from the trans

30 We have previously demonstrated that xenogeneic bone marrow engraftment and donor-specific to

31 on and in the facilitation of allogeneic and xenogeneic bone marrow engraftment.

32 and/or gammaDelta cell-mediated rejection of xenogeneic bone marrow.

33 increases the rapidity of PDLF attachment to xenogeneic bone replacement materials.

34 une response against the therapeutic and the xenogeneic carbohydrate galactose-alpha1-3-galactose, an

35 cellular responses that lead to rejection of xenogeneic cartilage are not well understood.

36 and may therefore contribute to rejection of xenogeneic cartilage.

37 on of KO mice with pig kidney membranes (ie, xenogeneic cell membranes expressing an abundance of alp

38 become key components for the development of xenogeneic cells and organs for human transplantation.

39 s play an important role in the rejection of xenogeneic cells and therefore represent a major obstacl

40 type; and improved survival of donor-derived xenogeneic cells at 2 and 4 wk in vivo.

41 contributes significantly to phagocytosis of xenogeneic cells by macrophages and suggest that genetic

42 y of CD47 may contribute to the rejection of xenogeneic cells by macrophages.

43 recent years, hepatic support systems using xenogeneic cells have been developed to support patients

44 nsplantation of a bioartificial adrenal with xenogeneic cells may be a treatment option for patients

45 on of coagulation pathways after exposure to xenogeneic cells or a vascularized xenograft.

46 The use of xenogeneic cells or tissues for tissue engineering appli

47 Even after immunization with Gal-bearing xenogeneic cells, mixed chimeras were devoid of anti-Gal

48 n the animals transplanted with syngeneic or xenogeneic cells, respectively.

49 ly high precursor frequency was detected for xenogeneic cellular responses in the rat anti-mouse comb

50 Furthermore, compared with fully xenogeneic chimeras (rat --> mouse), mixed xenogeneic ch

51 Mixed xenogeneic chimeras exhibit donor-specific humoral toler

52 y xenogeneic chimeras (rat --> mouse), mixed xenogeneic chimeras exhibit superior immunocompetence fo

53 In xenogeneic chimeras, T cell repertoire selection plays a

54 We have previously demonstrated that mixed xenogeneic chimerism and donor-specific T-cell tolerance

55 e ability of anti-CD40L mAb to promote mixed xenogeneic chimerism and donor-specific tolerance in B6

56 These results demonstrate that mixed xenogeneic chimerism establishes donor-specific humoral

57 Mixed allogeneic or xenogeneic chimerism indeed tolerizes both preexisting a

58 lability of human adrenal glands, sources of xenogeneic chromaffin cells will need to be identified i

59 Xenogeneic CM combined with tunnel technique leads to sa

60 were treated with the tunnel technique using xenogeneic CM.

61 +, CD8+, and CD4+CD8+ T cells in a rat/mouse xenogeneic co-culture.

62 Both xenogeneic collagen matrices combined with FDBA were eff

63 Considering xenogeneic collagen matrix (CM) and enamel matrix deriva

64 e purpose of this study is to determine if a xenogeneic collagen matrix (CM) might be as effective as

65 it-mouth design with CAF procedures or CAF + xenogeneic collagen matrix (CMX).

66 of inducing tolerance in a highly disparate xenogeneic combination and may have clinical potential t

67 lity has not been demonstrated in discordant xenogeneic combinations because of the difficulty in ach

68 e induction by mixed chimerism in discordant xenogeneic combinations.

69 ity induced by TCR adenoviruses required the xenogeneic constant regions and was mediated by CD8+ T c

70 ion in a pig-to-human model also reduces the xenogeneic consumption of human platelets by the porcine

71 the effect that these modifications have on xenogeneic consumption of human platelets in the absence

72 human CD19(+) B-lineage cells purified from xenogeneic cord blood stem cell/MS-5 murine stromal cell

73 We wished to determine the extent to which xenogeneic cornea fragments placed in the eyes of normal

74 The fate of xenogeneic cornea implants was assessed in mice immunize

75 Xenogeneic corneal fragments (guinea pig) are highly res

76 Xenogeneic corneal fragments implanted in the anterior c

77 By contrast, xenogeneic corneal fragments implanted in the anterior c

78 , we wished to determine the extent to which xenogeneic corneal fragments placed intraocularly in nor

79 Neutralization of IL-7 in xenogeneic cultures led to an increase in Ig light-chain

80 man CD19(+) cells developing in human/murine xenogeneic cultures show differential expression of the

81 Prime requirements for allogeneic, or xenogeneic, decellularized scaffolds are biocompatibilit

82 In this model of xenogeneic DNA immunization, the presence of an hgp100 h

83 ght to improve on this strategy by combining xenogeneic DNA vaccination with an agonist anti-glucocor

84 In contrast to allogeneic donor ECDI-SPs, xenogeneic donor ECDI-SPs induced production of xenodono

85 Xenogeneic donor-specific tolerance can be induced by tr

86 T cells and render recipients tolerant of a xenogeneic donor.

87 porcine endogenous retroviruses (PERV) from xenogeneic donors into humans has been widely debated.

88 d by human CTL (huCTL) vs allogeneic and pig xenogeneic EC targets.

89 re of immune-competent mice to injections of xenogeneic EC-TCPS induced vigorous host immunity.

90 Matrix-embedding protects xenogeneic ECs against immune reaction in naive mice and

91 tolerance in allogeneic and closely related xenogeneic (eg, rat-to-mouse) combinations, the ability

92 nse and the subsequent activation invoked by xenogeneic encounter.

93 c, nude rats injected intraperitoneally with xenogeneic endothelial cells (ECs) produce antibodies ag

94 redox systems may provide a means to protect xenogeneic endothelial cells from NK cell-mediated cytot

95 erated from monocytes under the influence of xenogeneic endothelial cells in the absence of exogenous

96 cells after co-culturing with allogeneic and xenogeneic endothelial cells, respectively.

97 An in vitro model of xenogeneic engraftment was established to identify inhib

98 d hematopoietic progenitor cells within this xenogeneic environment generated mature functional T cel

99 f specific T cell receptor-Vbeta occurs in a xenogeneic environment in a predictable fashion parallel

100 rtoire selection in tolerance induction in a xenogeneic environment.

101 characteristics that allow persistence in a xenogeneic environment.

102 d receptor in innate cellular recognition of xenogeneic epitopes.

103 Although a vigorous immune response to xenogeneic extracellular matrix biomaterials is expected

104 l biological scaffolds made of allogeneic or xenogeneic extracellular matrix derived from non-autolog

105 ival 3 weeks after injection of syngeneic or xenogeneic ferumoxides-labeled stem cells (cardiac-deriv

106 r tumorigenesis, we selectively targeted the xenogeneic form of survivin, a survival protein overexpr

107 ty was induced by DNA immunization against a xenogeneic form of TRP-2, but not against the syngeneic

108 induced by DEC205 targeting of the Ag in its xenogeneic form to maturing DCs.

109 an embryonic stem (hES) cells in defined and xenogeneic-free conditions will contribute substantially

110 ents a key step toward the fully defined and xenogeneic-free culture of hES cells.

111 C57BL/6 mice immunized with xenogeneic full-length hgp100 DNA were protected against

112 om autoimmune destruction and allogeneic and xenogeneic graft rejection.

113 s, and can instill long-lived allogeneic and xenogeneic graft tolerance.

114 t, in a preclinical humanized mouse model of xenogeneic graft-versus-host disease (GVHD), sGARP preve

115 onstrate that IL-15 but not IL-2 exacerbates xenogeneic graft-versus-host disease (X-GVHD) in severe

116 a-treated Treg in a humanized mouse model of xenogeneic graft-versus-host disease confirmed IFN-alpha

117 e induction of IFNgamma-secreting Tregs in a xenogeneic graft-versus-host disease model and in adopti

118 T cells and complete rescue from hyperacute xenogeneic graft-versus-host disease modeling early and

119 ls mediated tumor rejection without inducing xenogeneic graft-versus-host disease, thus resulting in

120 generated Tregs that consistently suppressed xenogeneic graft-vs-host disease in immunodeficient mice

121 munosuppression by human Tregs in a model of xenogeneic graft-vs.-host disease induced by the transfe

122 d could influence the findings; for example, xenogeneic grafts may not recognize host inhibitory sign

123 nd residual host immune function against the xenogeneic grafts results in defective development and m

124 to enhance the recruitment of host huTreg to xenogeneic grafts to regulate cell-mediated xenograft re

125 hway and promotes survival of allogeneic and xenogeneic grafts.

126 hat were capable of rejecting allogeneic and xenogeneic grafts.

127 Here, we report a novel, optimized NHP xenogeneic GVHD (xeno-GVHD) small animal model that reca

128 s expressing an irrelevant CAR at preventing xenogeneic GVHD caused by HLA-A2+ T cells.

129 R gene also conferred resistance to DEX in a xenogeneic GVHD model in sublethally irradiated NOD-scid

130 In a human xenogeneic GVHD model, human IL-21-secreting cells were

131 d prolonged time to fatal GVHD in an in vivo xenogeneic GVHD model.

132 iate into effectors able to mediate a potent xenogeneic GVHD.

133 Murine complement is capable of resisting xenogeneic hematopoietic engraftment through an antibody

134 A1CMAH knockout pigs were compared for their xenogeneic hepatic consumption of human platelets.

135 osuppression allows long-term functioning of xenogeneic hepatocyte retransplants and suggests that he

136 tocytes might address this problem; however, xenogeneic hepatocytes are thought to be functionally in

137 Following a single infusion, xenogeneic hepatocytes functioned for more than 80 days

138 The extent to which xenogeneic hepatocytes metabolize and excrete human orga

139 Transplants consisting of xenogeneic hepatocytes might overcome these problems, an

140 e-specific autoimmunity was seen only when a xenogeneic homolog of PAP was used as the immunogen.

141 generated by blastocyst complementation in a xenogeneic host.

142 s, and, as a result, are rapidly rejected in xenogeneic hosts.

143 ry considerably in their transmissibility to xenogeneic hosts.

144 hibiting allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses in vitro.

145 4IgG4 on allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses.

146 and the effects of costimulatory blockade on xenogeneic human anti-porcine T cell responses are also

147 Finally, CTLA4IgG4 prevented secondary xenogeneic human anti-porcine T cell responses.

148 ither tumor Valpha or Vbeta regions fused to xenogeneic human constant regions.

149 We used a xenogeneic human cord blood stem cell/murine stromal cel

150 ostimulatory pathways block the rejection of xenogeneic human embryonic-stem-cell-derived pancreatic

151 equivalents or normoglycemic rats with 5000 xenogeneic human islet equivalents.

152 Finally, huTreg partially suppressed xenogeneic human NK cell adhesion, NK cytotoxicity and d

153 fficient zygote genome editing technologies, xenogeneic human pluripotent stem cells may also open ne

154 We conclude that porcine Kupffer cells bind xenogeneic human RBC by recognition of a carbohydrate ep

155 Using xenogeneic (human) cells in immunosuppressed animals wit

156 is a murine T cell clone that recognizes the xenogeneic (human) class I MHC HLA-A2.1 molecule (A2) an

157 f primary GalT-KO skin grafts led to an anti-xenogeneic humoral response with no evidence for sensiti

158 ve-type CD4 cells (CD4/CD45RA ) and in vitro xenogeneic hyporesponsiveness were observed.

159 Porcine thymic tissue is able to induce xenogeneic hyporesponsiveness.

160 endothelial-mediated activation of allo- and xenogeneic immune cells.

161 not appear to differ in the nature of their xenogeneic immune response to the administered rabbit se

162 and exhibited similar levels of anti-rabbit xenogeneic immune response, the NZW mice had significant

163 Xenogeneic immunization with orthologous Ags induces can

164 ion between pig cell microchimerism and true xenogeneic infection.

165 occurred, and no evidence of transmission of xenogeneic infections was found.

166 tested this hypothesis in a human-into-mouse xenogeneic islet transplant model and validated the conc

167 In a rat-to-mouse xenogeneic islet transplant model, we show that rat ECDI

168 nal requirements for tolerance induction for xenogeneic islet transplantation using donor ECDI-SPs.

169 trategy for tolerance induction for clinical xenogeneic islet transplantation.

170 Xenogeneic islets are susceptible to complement-mediated

171 Xenogeneic islets implanted in nonimmunosuppressed rats

172 nologic challenges facing transplantation of xenogeneic islets, and the concerns regarding transmissi

173 mechanisms of post-transplant proteinuria in xenogeneic kidney transplantation and a potential strate

174 d the early development of proteinuria after xenogeneic kidney transplantation in baboons.

175 s combinations, its role in the rejection of xenogeneic marrow engraftment is unknown.

176 is to investigate the effect of filling with xenogeneic material the postextractive sockets of two su

177 results suggest that indirect recognition of xenogeneic MHC antigen plays a predominant role in graft

178 cells elicit a vigorous response to allo- or xenogeneic MHC class I molecules.

179 At present, it is not clear whether xenogeneic MHC molecules are recognized by T cells direc

180 survival of T cells positively selected by a xenogeneic MHC, as well as incomplete intrathymic deleti

181 ed decreased signal intensity not only for a xenogeneic mismatch in species but, surprisingly, also f

182 Human anti-porcine xenogeneic MLRs were blocked by CTLA4IgG4, but only mini

183 vitro, as well as engraftment potential in a xenogeneic model after partial myeloablation.

184 ited antileukemic activity in vivo against a xenogeneic model of disseminated AML.

185 t efficiency have been explored in a primate xenogeneic model of in utero hematopoietic stem cell tra

186 the induction of tolerance in the discordant xenogeneic model of pig-to-rodent thymic transplantation

187 ferent cellular mechanisms in allogeneic and xenogeneic model systems.

188 In the xenogeneic model, we quantified islet transplant exosome

189 profile of human HSC engraftment in a living xenogeneic model.

190 r differentiation of the human cells in this xenogeneic model.

191 Moreover, in a xenogeneic mouse model of breast carcinoma, in vivo trea

192 ablished from EBV-infected B-cell lines in a xenogeneic mouse model of PTLD.

193 on in the presence of immunosuppression in a xenogeneic mouse model.

194 f HER2/neu-positive human breast tumors in a xenogeneic mouse model.

195 Xenogeneic mouse models are broadly used to study human

196 Two xenogeneic mouse models bearing intracranial human GBMs

197 his study reports the establishment of fully xenogeneic mouse-->rat multilineage chimeras and evaluat

198 Fully xenogeneic multilineage bone marrow chimerism was produc

199 sus-leukemia (GVL) effects in allogeneic and xenogeneic murine GVHD models.

200 T-cell function is severely impaired in the xenogeneic murine microenvironment.

201 further genetic modification of the pig, and xenogeneic NK cell recognition and activation may be inh

202 irus (EBV)-driven human B-cell lymphoma in a xenogeneic NOD/SCID/IL2rg(null) mouse model.

203 of JAM-C in homing of human B cells, using a xenogeneic nonobese diabetic/severe combined immunodefic

204 of T cells (and T cell subsets) after either xenogeneic or allogeneic activation in vitro or in vivo.

205 issue because the ability to implant either xenogeneic or allogeneic cells would greatly enhance the

206 ornea upon grafting to LSC-deficient mice in xenogeneic or syngeneic transplantation models.

207 tiple rounds of stimulation with allogeneic, xenogeneic, or antigen-pulsed autologous antigen-present

208 Immunization of mice with plasmids encoding xenogeneic orthologues of tumor differentiation antigens

209 Expression of HLA-G on PAECs protected xenogeneic PAECs against human polyclonal NK cell-mediat

210 one Ceropithecus aethiops) were treated with xenogeneic pancreatic islets (Macaca mulatta).

211 uch as eptifibatide, interfere directly with xenogeneic PBPC-platelet interactions and may further am

212 bile acids in patient serum increases during xenogeneic perfusion for unknown reasons.

213 Xenogeneic peripheral blood chimerism was assessed after

214 methods for induction of immune tolerance to xenogeneic pig antigens.

215 prolong allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice

216 prolongs allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice

217 Highly disparate xenogeneic pig skin graft tolerance and efficient repopu

218 Highly disparate xenogeneic pig skin graft tolerance can be achieved by g

219 een with either allogeneic (rat-into-rat) or xenogeneic (pig-into-rat) transplants over 28 days, comp

220 A maternal immune response to the xenogeneic placental antigen was shown by the presence o

221 d ASGR1 expression as well as ASGR1-mediated xenogeneic platelet phagocytosis in vitro and ex vivo on

222 tiated cell lines are capable of recognizing xenogeneic porcine aortic endothelial cells in a calcium

223 rge-animal model raises the possibility that xenogeneic porcine islet tissue will also survive in hum

224 is potent enough to prevent the rejection of xenogeneic porcine islets in a large-animal model.

225 CD4 T cells are specifically tolerant of the xenogeneic porcine thymus donor and the recipient, but a

226 ll-depleted, thymectomized mice grafted with xenogeneic porcine thymus tissue.

227 However, in the xenogeneic rat-to-mouse combination, additional anti-Thy

228 he hypothesis that porcine sialoadhesin is a xenogeneic receptor that mediates porcine macrophage bin

229 poietic cell engraftment in highly disparate xenogeneic recipients remains unclear.

230 swine-specific tolerance in widely disparate xenogeneic recipients, this study aimed to achieve long-

231 sed regimen was not effective for preventing xenogeneic rejection.

232 l ignorance and experience largely mitigated xenogeneic rejection.

233 ever, the immunogenicity of cells expressing xenogeneic reporter constructs limits their survival and

234 egs may be required to suppress the stronger xenogeneic response.

235 CD4 T cells and the indirect pathway in the xenogeneic response.

236 Both discordant and concordant xenogeneic responses are dominated by humoral immunity.

237 uTreg) suppress CD4+ T cell-mediated antipig xenogeneic responses in vitro and might therefore be use

238 fference between human T cell allogeneic and xenogeneic responses in vivo.

239 Xenogeneic responses were unique in the continued expres

240 ccommodation has been widely investigated in xenogeneic responses.

241 repared from monocytes ex vivo without using xenogeneic serum and may be used for immunotherapy.

242 As a consequence, thymopoiesis in this xenogeneic setting began by weeks 4-6, peaked at mo 3, a

243 derstanding the biochemistry of H-NS and how xenogeneic silencing affects bacterial evolution.

244 standing of the mechanisms and importance of xenogeneic silencing and counter-silencing in the succes

245 Xenogeneic silencing of horizontally-acquired genes by H

246 Most notably, xenogeneic silencing proteins bind incoming DNA that has

247 ession of foreign DNA in a process known as 'xenogeneic silencing.' Counter-silencing by a variety of

248 kin did not lead to accelerated rejection of xenogeneic skin.

249 opoietic engraftment across highly disparate xenogeneic species barriers poses a major obstacle to ex

250 ing T cell tolerance across highly disparate xenogeneic species barriers.

251 ant in the rejection of solid organs in some xenogeneic species combinations, its role in the rejecti

252 orcine donor responses in a highly disparate xenogeneic species.

253 This could present major limitations to xenogeneic stem cell transplantation as an approach to t

254 use of homologous stem cells, allogeneic or xenogeneic stem cells have been studied extensively in e

255 ated inflammatory reaction to allogeneic and xenogeneic stem cells may elicit a spectrum of effects,

256 response that is exaggerated with the use of xenogeneic stem cells.

257 ming comparing activation with allogeneic or xenogeneic stimulators.

258 fluence T cell repertoire in response to the xenogeneic stimulus.

259 n leukocyte antigen (HLA) antibodies against xenogeneic swine leukocyte antigen (SLA) antigens.

260 well as the nature of Th unresponsiveness to xenogeneic (swine) antigens induced by Ts.

261 Using a xenogeneic system, here we define the bioenergetic chang

262 In this xenogeneic system, human mesenchymal stem cells engrafte

263 However, the xenogeneic T cell precursor frequency was found to be ma

264 litates metastasis in both the syngeneic and xenogeneic (T and B lymphocyte deficient) systems.

265 ted with an increased spontaneous killing of xenogeneic target cells.

266 2-Dd, might display public specificities for xenogeneic target structures.

267 tudies suggest that mouse NK cells recognize xenogeneic targets in a strain-specific manner, implicat

268 autologous fibroblasts and rVVenv-expressing xenogeneic targets similarly, suggesting a lack of genet

269 ive selection is mediated exclusively by the xenogeneic thymic MHC.

270 Our results support the interpretation that xenogeneic thymic transplantation is a feasible strategy

271 normal mice usually remain healthy following xenogeneic thymic transplantation, thymus-grafted congen

272 Transplantation of xenogeneic thymus tissue allows xenograft tolerance indu

273 Xenogeneic thymus transplantation is an effective approa

274 The survival of xenogeneic tissue in the absence of immunosuppression in

275 Mice were implanted s.c. with xenogeneic tissue, syngeneic tissue, or SIS, and the gra

276 ra-abdominal testis supports the survival of xenogeneic tissue.

277 Because xenogeneic tissues are subject to vigorous immune reject

278 Xenogeneic tissues induce vigorous T cell immunity, refl

279 haracterize further the cellular response to xenogeneic tissues, we used the intracellular fluorescen

280 CD4 T-cell reconstitution and xenogeneic tolerance is achieved in T cell-depleted, thy

281 econstitute mouse CD4+ T cells and to induce xenogeneic tolerance to donor pig skin grafts.

282 LIV in the mediastinum, suggesting that full xenogeneic tolerance was not achieved in euthymic mice.

283 t before syngeneic, suboptimal syngeneic, or xenogeneic transplant exhibited superior function compar

284 ma and ascites formation in an athymic mouse xenogeneic transplant model of ovarian cancer.

285 rent research efforts in both allogeneic and xenogeneic transplantation are presented and discussed.

286 ed from the islets of the pancreas can cross xenogeneic transplantation immune barriers, induce tissu

287 In conclusion, xenogeneic transplantation of human PBSCs into NOD/SCID

288 lls, tissues, and organs after allogeneic or xenogeneic transplantation.

289 and 3) models of syngeneic, allogeneic, and xenogeneic transplantation.

290 t preservation in syngeneic, allogeneic, and xenogeneic transplantation.

291 of T cell-mediated immune responses against xenogeneic transplants.

292 The expression of xenogeneic TRIM5alpha proteins can restrict infection in

293 The results showed that the xenogeneic tumors can grow and metastasize.

294 The eradication of xenogeneic tumors in a murine environment shows that the

295 Rejection of xenogeneic tumors was also T-cell dependent as demonstra

296 peutic efficacy in mice with RL cell-derived xenogeneic tumors.

297 luenza virus type 1 (Sendai virus [SV]) as a xenogeneic vector to deliver the G glycoprotein of RSV.

298 Differences in xenogeneic versus allogeneic activation profiles exist t

299 linical efficacy of synthetic, allogeneic or xenogeneic vessels has been limited by thrombosis, rejec

300 llogeneic BALB/c or phylogenetically related xenogeneic WF rat stimulator cells while having undetect